Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05080 | A02 | 2226472 | C | T | missense_variant | MODERATE | c.433C>T|p.Leu145Phe |
S58 |
2 | BAA02g05080 | A02 | 2227096 | C | T | missense_variant&splice_region_variant | MODERATE | c.496C>T|p.Leu166Phe |
S131 |
3 | BAA02g05080 | A02 | 2227127 | G | A | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S223 |
4 | BAA02g05080 | A02 | 2228359 | C | T | downstream_gene_variant | MODIFIER | c.*1204C>T| |
S71 |
5 | BAA02g05080 | A02 | 2229920 | G | A | downstream_gene_variant | MODIFIER | c.*2765G>A| |
S82 S92 |